AUTO LENSMETER

GUDID 04582273612402

100V

TOMEY CORPORATION.

Automated lensmeter Automated lensmeter Automated lensmeter Automated lensmeter Automated lensmeter Automated lensmeter Automated lensmeter Automated lensmeter
Primary Device ID04582273612402
NIH Device Record Key7ecea8af-1bf1-4a6a-ab6c-1f4d0403a8e8
Commercial Distribution StatusIn Commercial Distribution
Brand NameAUTO LENSMETER
Version Model NumberTL-100
Company DUNS696280002
Company NameTOMEY CORPORATION.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS104582273612402 [Primary]
GS104582273612402 [Primary]
GS104582273612402 [Primary]
GS104582273612402 [Primary]
GS104582273612402 [Primary]
GS104582273612402 [Primary]
GS104582273612402 [Primary]
GS104582273612402 [Primary]

FDA Product Code

HLMInstrument, Measuring, Lens, Ac-Powered
HLMInstrument, Measuring, Lens, Ac-Powered
HLMInstrument, Measuring, Lens, Ac-Powered
HLMInstrument, Measuring, Lens, Ac-Powered
HLMInstrument, Measuring, Lens, Ac-Powered
HLMInstrument, Measuring, Lens, Ac-Powered
HLMInstrument, Measuring, Lens, Ac-Powered
HLMInstrument, Measuring, Lens, Ac-Powered

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-11-09
Device Publish Date2020-10-30

On-Brand Devices [AUTO LENSMETER]

04582273612686100V
04582273612655100V
04582273612402100V

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